Determining Subarctic Peatland Vegetation Using an Unmanned Aerial System (UAS) by Palace, Michael, Herrick, Christina, DelGreco, Jessica, Finnell, Daniel, Garnello, Anthony, McCalley, Carmody, McArthur, Kellen, Sullivan, Franklin, Varner, Ruth

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Perioperative Management and Outcomes of Esophageal Atresia and Tracheoesophageal Fistula by Lal, Dave R, Gadepalli, Samir K, Downard, Cynthia D, Ostlie, Daniel J, Minneci, Peter C, Swedler, Ruth M, Chelius, Thomas, Cassidy, Laura, Rapp, Cooper T, Sato, Thomas T, Deans, Katherine J, Fallat, Mary E, Finnell, S Maria E, Helmrath, Michael A, Hirschl, Ronald B, Kabre, Rashmi S, Leys, Charles M, Mak, Grace, Minneci, Peter C, Saito, Jacqueline M, St. Peter, Shawn D, von Allmen, Daniel

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Amniotic fluid-derived stem cells: potential factories of natural and mimetic strategies for congenital malformations by Fonteles, Cristiane S R, Enterria-Rosales, Julia, Lin, Ying, Steele, John W, Villarreal-Leal, Ramiro A, Xiao, Jing, Idowu, Daniel I, Burgelin, Beck, Wlodarczyk, Bogdan J, Finnell, Richard H, Corradetti, Bruna

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Dolutegravir induces FOLR1 expression during brain organoid development by Caiaffa, Carlo Donato, Tukeman, Gabriel, Delgado, Christian Zevallos, Ambekar, Yogeshwari S, Mekonnen, Taye T, Singh, Manmohan, Rodriguez, Victoria, Ricco, Emily, Kraushaar, Daniel, Aglyamov, Salavat R, Scarcelli, Giuliano, Larin, Kirill V, Finnell, Richard H, Cabrera, Robert M

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Developments in our understanding of the genetic basis of birth defects by Webber, Daniel M., MacLeod, Stewart L., Bamshad, Michael J., Shaw, Gary M., Finnell, Richard H., Shete, Sanjay S., Witte, John S., Erickson, Stephen W., Murphy, Linda D., Hobbs, Charlotte

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Exome sequencing identifies genetic variants in anophthalmia and microphthalmia by Li, Jingjing, Yang, Wei, Wang, Yuejun Jessie, Ma, Chen, Curry, Cynthia J., McGoldrick, Daniel, Nickerson, Deborah A., Chong, Jessica X., Blue, Elizabeth E., Mullikin, James C., Reefhuis, Jennita, Nembhard, Wendy N., Romitti, Paul A., Werler, Martha M., Browne, Marilyn L., Olshan, Andrew F., Finnell, Richard H., Feldkamp, Marcia L., Pangilinan, Faith, Almli, Lynn M., Bamshad, Mike J., Brody, Lawrence C., Jenkins, Mary M., Shaw, Gary M.

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Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children by Pitsava, Georgia, Feldkamp, Marcia L., Pankratz, Nathan, Lane, John, Kay, Denise M., Conway, Kristin M., Shaw, Gary M., Reefhuis, Jennita, Jenkins, Mary M., Almli, Lynn M., Olshan, Andrew F., Pangilinan, Faith, Brody, Lawrence C., Sicko, Robert J., Hobbs, Charlotte A., Bamshad, Mike, McGoldrick, Daniel, Nickerson, Deborah A., Finnell, Richard H., Mullikin, James, Romitti, Paul A., Mills, James L.

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Precision medicine within health professions education: Defining a research agenda for emergency medicine using a foresight and strategy technique (FaST) review by Chan, Teresa M, Thoma, Brent, Finnell, John T, Gordon, Bradley D, Farrell, Susan, Pusic, Martin, Cabrera, Daniel, Gisondi, Michael A, Caretta-Weyer, Holly A, Stave, Christopher, Ankel, Felix

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Analysis of archived residual newborn screening blood spots after whole genome amplification by Cantarel, Brandi L, Lei, Yunping, Weaver, Daniel, Zhu, Huiping, Farrell, Andrew, Benstead-Hume, Graeme, Reese, Justin, Finnell, Richard H

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Developmental consequences of abnormal folate transport during murine heart morphogenesis by Tang, Louisa S., Wlodarczyk, Bogdan J., Santillano, Daniel R., Miranda, Rajesh C., Finnell, Richard H.

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Fetal antiepileptic drug exposure: Adaptive and emotional/behavioral functioning at age 6years by Cohen, Morris J., Meador, Kimford J., Browning, Nancy, May, Ryan, Baker, Gus A., Clayton-Smith, Jill, Kalayjian, Laura A., Kanner, Andres, Liporace, Joyce D., Pennell, Page B., Privitera, Michael, Loring, David W.

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Development of a Multi-Institutional Clinical Research Consortium for Pediatric Surgery by Hirschl, Ronald B, Minneci, Peter, Gadepalli, Samir, Saito, Jacqueline M

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Erratum to: Folate-Regulated Changes in Gene Expression in the Anterior Neural Tube of Folate Binding Protein-1 (Folbp1)-Deficient Murine Embryos by Spiegelstein, Ofer, Cabrera, Robert M., Bozinov, Daniel, Wlodarczyk, Bogdan, Finnell, Richard H.

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Exome sequencing identifies variants in infants with sacral agenesis by Pitsava, Georgia, Feldkamp, Marcia L., Pankratz, Nathan, Lane, John, Kay, Denise M., Conway, Kristin M., Hobbs, Charlotte, Shaw, Gary M., Reefhuis, Jennita, Jenkins, Mary M., Almli, Lynn M., Moore, Cynthia, Werler, Martha, Browne, Marilyn L., Cunniff, Chris, Olshan, Andrew F., Pangilinan, Faith, Brody, Lawrence C., Sicko, Robert J., Finnell, Richard H., Bamshad, Michael J., McGoldrick, Daniel, Nickerson, Deborah A., Mullikin, James C., Romitti, Paul A., Mills, James L., Brody, Lawrence C., Browne, Marilyn L., Feldkamp, Marcia L., Hobbs, Charlotte, Jenkins, Mary M., Olshan, Andrew F., Reefhuis, Jennita, Romitti, Paul A., Shaw, Gary M., Werler, Martha, Almli, Lynn M., Browne, Marilyn L., Conway, Kristin M., Feldkamp, Marcia L., Finnell, Richard H., Hobbs, Charlotte, Jenkins, Mary M., Moore, Cynthia, Olshan, Andrew F., Reefhuis, Jennita, Keegan, Romitti, Paul A., Shaw, Gary M., Werler, Martha, Bamshad, Michael J., Brody, Lawrence C., Kay, Denise M., McGoldrick, Daniel, Mullikin, James C., Nickerson, Deborah A., Pangilinan, Faith, Sicko, Robert J., Lane, John, Pankratz, Nathan, Bamshad, Michael J., Brody, Lawrence C., Feldkamp, Marcia L., Kay, Denise M., Lane, John, McGoldrick, Daniel, Mills, James L., Nickerson, Deborah A., Pankratz, Nathan, Pitsava, Georgia, Romitti, Paul A., Sicko, Robert J., Pitsava, Georgia, Feldkamp, Marcia L., Kay, Denise M., Lane, John, Mills, James L., Pankratz, Nathan, Pangilinan, Faith, Romitti, Paul A., Almli, Lynn M., Bamshad, Michael J., Brody, Lawrence C., Conway, Kristin M., Cunniff, Chris, Finnell, Richard H., Hobbs, Charlotte, Jenkins, Mary M., McGoldrick, Daniel, Mullikin, James C., Nickerson, Deborah A., Olshan, Andrew F., Reefhuis, Jennita, Keegan, Browne, Marilyn L., Canfield, Shaw, Gary M., Sicko, Robert J., Mills, James L., Romitti, Paul A.

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Evaluating congruence between laboratory LOINC value sets for quality measures, public health reporting, and mapping common tests by Wu, Jianmin, Finnell, John T, Vreeman, Daniel J

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Arsenic-induced gene expression changes in the neural tube of folate transport defective mouse embryos by Wlodarczyk, Bogdan J., Cabrera, Robert M., Hill, Denise S., Bozinov, Daniel, Zhu, Huiping, Finnell, Richard H.

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Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data by Jenkins, Mary M., Almli, Lynn M., Pangilinan, Faith, Chong, Jessica X., Blue, Elizabeth E., Shapira, Stuart K., White, Janson, McGoldrick, Daniel, Smith, Joshua D., Mullikin, James C., Bean, Christopher J., Nembhard, Wendy N., Lou, Xiang‐Yang, Shaw, Gary M., Romitti, Paul A., Keppler‐Noreuil, Kim, Yazdy, Mahsa M., Kay, Denise M., Carter, Tonia C., Olshan, Andrew F., Moore, Kristin J., Nascone‐Yoder, Nanette, Finnell, Richard H., Lupo, Philip J., Feldkamp, Marcia L., Nickerson, Deborah A., Bamshad, Michael J., Brody, Lawrence C., Reefhuis, Jennita

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Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk by Morin, Isabelle, Devlin, Angela M, Leclerc, Daniel, Sabbaghian, Nelly, Halsted, Charles H, Finnell, Richard, Rozen, Rima

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Folate transport gene inactivation in mice increases sensitivity to colon carcinogenesis by MA, David W. L, FINNELL, Richard H, BOZINOV, Daniel, LUPTON, Joanne R, CHAPKIN, Robert S, DAVIDSON, Laurie A, CALLAWAY, Evelyn S, SPIEGELSTEIN, Ofer, PIEDRAHITA, Jorge A, SALBAUM, J. Michael, KAPPEN, Claudia, WEEKS, Brad R, JAMES, Jill

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Differentially expressed genes in embryonic cardiac tissues of mice lacking Folr1 gene activity by Zhu, Huiping, Cabrera, Robert M, Wlodarczyk, Bogdan J, Bozinov, Daniel, Wang, Deli, Schwartz, Robert J, Finnell, Richard H

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